Dear Listers,
to clarify the HV vs. Gain on FluoView FV1000 topic and to follow Stanislav Vithas request for someone from Olympus to answer: 1. Adjust HV of the PMT. This regulates how many counts are generated by a photon hitting the PMT. When you have a weak sample with a good S/N you can raise the HV to a value where the brightest Point on your image generates 4095 counts, therefore using the complete dynamic range. (Of course also with a strong sample it is desirable to use the complete dynamic range for your sample, it simple generates a better data-quality). But be aware: If you raise the HV too much you reach the non-linear range of the PMT, leading to an unequal amplification of areas of different brightness. 2. The Gain is an alternative way to facilitate the full dynamic range of the AD- Converter. To give an example: By using only the HV your sample has intensity values from 0-1000 counts, rising the HV to top end would take you into the nonlinear range of the PMT. If this signal is converted by the ADC, you do not use the whole dynamic range of 4096. If you add a Gain of e.g. 4, you get everything multiplied by 4 – the PMT noise as well as the actual analog signal. The PMT noise will be higher, but now you can use a much larger dynamic range – up to 4095 without sacrificing the linearity of the image. Another advantage is that the quantization noise will be smaller in comparison to the signal. Plainly, if you have a weak sample that can not be imaged with the full dynamic range in the linear range using the HV, you can use Gain to amplify the image and to keep the HV in the linear range. If you don´t care about using the full dynamic range, there is no need to use the Gain. Best regards Florian Eich Olympus Life Science Europa GmbH |
Julian Smith III |
Thanks for the very clear explanation of the difference!
How does one determine where one's PMT's become non-linear? Julian Florian Eich wrote: > Dear Listers, > to clarify the HV vs. Gain on FluoView FV1000 topic and to follow Stanislav > Vithas request for someone from Olympus to answer: > > 1. Adjust HV of the PMT. This regulates how many counts are generated by a > photon hitting the PMT. When you have a weak sample with a good S/N you > can raise the HV to a value where the brightest Point on your image generates > 4095 counts, therefore using the complete dynamic range. (Of course also > with a strong sample it is desirable to use the complete dynamic range for your > sample, it simple generates a better data-quality). > But be aware: If you raise the HV too much you reach the non-linear range of > the PMT, leading to an unequal amplification of areas of different brightness. > > 2. The Gain is an alternative way to facilitate the full dynamic range of the AD- > Converter. To give an example: By using only the HV your sample has intensity > values from 0-1000 counts, rising the HV to top end would take you into the > nonlinear range of the PMT. If this signal is converted by the ADC, you do not > use the whole dynamic range of 4096. If you add a Gain of e.g. 4, you get > everything multiplied by 4 – the PMT noise as well as the actual analog signal. > The PMT noise will be higher, but now you can use a much larger dynamic > range – up to 4095 without sacrificing the linearity of the image. Another > advantage is that the quantization noise will be smaller in comparison to the > signal. > > Plainly, if you have a weak sample that can not be imaged with the full > dynamic range in the linear range using the HV, you can use Gain to amplify > the image and to keep the HV in the linear range. If you don´t care about > using the full dynamic range, there is no need to use the Gain. > > Best regards > Florian Eich > Olympus Life Science Europa GmbH > > -- Julian P.S. Smith III Director, Winthrop Microscopy Facility Dept. of Biology Winthrop University 520 Cherry Rd. Rock Hill, SC 29733 803-323-2111 x6427 (vox) 803-323-3448 (fax) 803-524-2347 (cell) |
Barbara Foster |
Hi, Julian
One exercise we used to do when I was supporting the short-lived microspectrometry program at Cambridge/Reichert Jung was to use a 4 quadrant calibration system. It was actually a fluorescent plate with neutral density material of 3 different, known optical densities coated on it. We would take a reading of the clear + 3 nd filter areas then plot it. It was pretty evident where the PMT became non-linear. That information was automatically fed into the system and became part of the system correction algorithm. Hope this is helpful. Barbara Foster, President Microscopy/Microscopy Education 7101 Royal Glen Trail, Suite A McKinney TX 75070 P: (972)924-5310 Skype: fostermme W: www.MicroscopyEducation.com NEWS! Visit the NEW and IMPROVED www.MicroscopyEducation.com! And don't forget: MME is now scheduling customized, on-site courses through March 2009. Call me for a free assessment and quote. At 07:27 AM 10/8/2008, you wrote: Thanks for the very clear explanation of the difference! |
G. Esteban Fernandez |
If you lack samples of known OD you can vary fluorescence intensity by varying the intensity of the excitation laser light, then plot fluorescence vs. laser % to check linearity. This assumes that the AOTF that regulates laser power is linear but this is a reasonable assumption, see "Quantitative Fluorescence", Ch. 14 in Optical Imaging Techniques in Cell Biology, by Guy Cox (2007).
-Esteban
On Wed, Oct 8, 2008 at 12:12 PM, Barbara Foster <[hidden email]> wrote:
-- G. Esteban Fernandez, Ph.D. Associate Director Molecular Cytology Core Facility University of Missouri 120 Bond Life Sciences Center Columbia, MO 65211 http://www.biotech.missouri.edu/mcc/ 573-882-4895 573-884-9395 fax |
Mark Cannell |
In reply to this post by Julian Smith III
I think this question has been addressed incorrectly IMHO.
Changing the digital gain does not do anything to the recorded signal except scale it up -noise and all. (IMHO, this a useless feature and I have never ever used it on _any _ confocal I've used). Now the pmt is intrinsically a *very* linear device. This was well established in the 1960's by extensive tests by EMI. The linearity of pmts was essential for the precise stellar measurements being made by astronomers. Non-linear behavior may be introduced by poor application design, in particular dynode chain design leaving to dynode voltage droop or local overload of electrodes (cathode, dynodes &/or anode) and exceeding manufacturer limits (which will burn the coatings). In fact, the pmt itself is generally more linear than the current-to-voltage amplifier and A/D converter -provided you do not exceed design limits. A few numbers may help make this clear. If you want < 0.1% non-linearity total tube current cannot exceed 0.1% of dynode chain current which is typically 1mA (it may be somewhat less than this as gain is only linear on a log log plot only and is different for each tube). This implies a maximum acceptable tube current of ~1uA for our application design point. Assuming a maximum design tube gain of 10^7 (actual tubes can go higher than this), this gives a detected photon flux = 0.1pA which is about 6 x 10^5 photoelectrons per second. As you reduce operating voltage, the tube gain goes down and the tube current falls in parallel. So if the manufacturers have correctly set the A/D converter system gain up so that the detector is linear to 0.1% at maximum gain then this will NOT change with pmt voltage (unless you can exceed the maximum design voltage/gain for the system). This also means that regardless of the scene brightness, the maximum non-linearity is 0.1% provided no pixels are saturated. At a dwell time of 1us per pixel this maximum gain implies only 0.6 counts per pixel (/us) for this design example (I suggest there is NO point scaling this value to 4096...). The bottom line is that detector linearity will not change with pmt votage if you always have the same A/D converter gain. Post multiplication of the A/D value does nothing to the scene information. In dim images where high gain is used, 8 bit recording is perfectly adequate ('cos less than 100 photoelectrons per pixel) and gives smaller file sizes. If the scene has a dynamic range of 4000 peak average photon count per pixel would then have to be >1000 (from almost no saturated pixels). This represents a huge photon flux at a 1us dwell time but might be achieved with slower scans. (It is less clear whether it would be better to scan fast and average). If there is serious non-linearity in the detector of the Olympus, it can only be due to bad electrical design (and it needs to be fixed by redesign) and changing pmt voltage will not alter it. If the light is too concentrated on the photocathode so that local saturation occurs then that would need fixing too. I suspect that neither of these problems are actually present and the original poster is in error. All 3 confocal systems (non-Olympus) I have seen inside have had non-zener controlled k-d1 dynode steps implying they are being used far from currents where dynode droop (and linearity) becomes a problem. My advice is to ignore the digital gain and set pmt voltage to give the desired gain -and remember to set the black level correctly or your image really will be non-linear. My 20c Regards Mark Cannell Julian Smith III wrote: > Thanks for the very clear explanation of the difference! > How does one determine where one's PMT's become non-linear? > Julian > > Florian Eich wrote: >> Dear Listers, >> to clarify the HV vs. Gain on FluoView FV1000 topic and to follow >> Stanislav Vithas request for someone from Olympus to answer: >> >> 1. Adjust HV of the PMT. This regulates how many counts are generated >> by a photon hitting the PMT. When you have a weak sample with a good >> S/N you can raise the HV to a value where the brightest Point on your >> image generates 4095 counts, therefore using the complete dynamic >> range. (Of course also with a strong sample it is desirable to use >> the complete dynamic range for your sample, it simple generates a >> better data-quality). >> But be aware: If you raise the HV too much you reach the non-linear >> range of the PMT, leading to an unequal amplification of areas of >> different brightness. >> 2. The Gain is an alternative way to facilitate the full dynamic >> range of the AD- >> Converter. To give an example: By using only the HV your sample has >> intensity values from 0-1000 counts, rising the HV to top end would >> take you into the nonlinear range of the PMT. If this signal is >> converted by the ADC, you do not use the whole dynamic range of 4096. >> If you add a Gain of e.g. 4, you get everything multiplied by 4 – the >> PMT noise as well as the actual analog signal. The PMT noise will be >> higher, but now you can use a much larger dynamic range – up to 4095 >> without sacrificing the linearity of the image. Another advantage is >> that the quantization noise will be smaller in comparison to the signal. >> Plainly, if you have a weak sample that can not be imaged with the >> full dynamic range in the linear range using the HV, you can use >> Gain to amplify the image and to keep the HV in the linear range. If >> you don´t care about using the full dynamic range, there is no need >> to use the Gain. >> >> Best regards >> Florian Eich >> Olympus Life Science Europa GmbH >> >> > > |
Florian Eich |
In reply to this post by Julian Smith III
Dear Listers,
maybe my latest post was not clear enough, or even misleading, I am very sorry for the inconvenience. To answer on the comments on HV vs gain topic and the following posts about PMT linearity: In my previous post I wrote “If you raise HV too much you reach the non- linear range of the PMT.” I guess that my improper and imprecise use of the term linearity in this context caused confusion. Saturation would have been the right term. Please accept my excuses. The PMTs in FluoView FV1000 work in their linear range. A linear relation of gain vs supply voltage on the PMT is given from 300 to 1250V. I tried to attach a graph, but list-rules prevent this. Feel free to contact me to get the graph. Please do not mistake this for the gain which you can modulate in the software. The gain you modulate in the software is an amplification of the signal AFTER the PMT but BEFORE the AD-Converter, so, like Marc Cannell rightly stated, is a pure amplification by a set factor. But you do not multiply the quantisation error of the ADC because the amplification takes place before AD conversion. I hope this answered any open questions. Best Regards Florian Eich Olympus Life Science Europa GmbH |
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